Canonical Allele Identifier: PA658800682
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 498446
ClinVar RCV Id: RCV000593474 RCV001143465 RCV003889930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Arg29Trp
CA1592724
NM_001029883.3:c.85C>T